ImpactLife
Form 483 issued July 3, 2025 · Urbana, Illinois
- Inspection
- Jun 30 – Jul 3, 2025
- Investigator
- Zoey A. Trombley
- Observations
- 1
- Pages
- 3
- FEI number
- 1470270
In short: On July 3, 2025, FDA issued a Form 483 with 1 observation to ImpactLife in Urbana, Illinois (FEI 1470270) after an inspection that ran Jun 30 – Jul 3, 2025. The investigator was Zoey A. Trombley. Most observations concern biologics CGMP; the most-cited regulation is 21 CFR 606.170 (adverse reaction file).
At a glance
1 of 1 observations on this 483 concern biologics cgmp.
Most cited: 21 CFR 606.170(a) (1×)
What FDA observed
Preview: the opening words of each observation- 01
Written reports of investigations of adverse reactions, including conclusions and follow up, are…
This inspection in context
Zoey A. Trombley
1 document · 2025
Cites 606.170(a) (adverse reaction file) more than any other section. Most of their documents are for sites in Illinois.
The firmImpactLife history
The site's inspection history, in date order.
Similar 483sOther sites cited under 606.170(a)
See how FDA wrote the same problem up elsewhere.
Questions about this 483
What did FDA find at ImpactLife?
FDA listed 1 observation on this Form 483, mostly about biologics CGMP. The most-cited regulation is 21 CFR 606.170 (adverse reaction file). The opening words of each observation are shown on this page.
Who inspected ImpactLife?
Zoey A. Trombley is named on this Form 483, for the inspection of Jun 30 – Jul 3, 2025. Each investigator has a profile showing what they cite most.
When was ImpactLife inspected by FDA?
The inspection ran Jun 30 – Jul 3, 2025, and the Form 483 is dated July 3, 2025.
How do I get the full Form 483 for ImpactLife?
Download the original PDF from FDA Intel for $99, with no subscription. Your first Form 483 or letter is on us. You also get an invoice PDF with the order.